NCT02899520终止不适用
Evaluation of Programs of Reeducation for Urinary Incontinence in Woman
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- Hopital Foch
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- USP (Urinary Symptoms Profile) score
研究概览
简要总结
The objective of this study is to compare two methods of pelvic floor muscle training: reference method versus CMP ® method ( (Connaissance et Maîtrise de Périnée : Knowledge and Control of Perineum)
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Patients more than 18 years old and less than 75 years
- •Patients presenting an urinary incontinence of effort or mixed symptomatic associated with a pelvic statics disorder
- •Patients with a perineale reeducation prescription
- •Patients affiliated to a national insurance scheme or benefiting from such a program
- •Patients having given her written consent form
排除标准
- •Nulliparous woman
- •Patients already operated for their incontinence
- •Patients with a prolapse of higher level at the stage II of the classification POP-Q (Pelvic Organ Prolapse Quantification)
- •Pregnant women
- •Patients presenting an associated anal incontinence,
- •Patients presenting a cancellation (section of marrow, syringomyelia for example) or an inversion of perineum control
- •Patients having given birth less than 6 months before the care
- •Patients having benefited from a pelvi-périnéale reeducation in the previous 12 months,
- •Patients presenting psychiatric disease
- •Patients presenting a vaginismus,
- •Patients presenting a contraindication to the practice of the electrostimulation.
研究组 & 干预措施
Group A
Active Comparator
Reference method
干预措施: Reference method (Other)
Group B
Experimental
CMP ® method (Knowledge and Control of Perineum)
干预措施: CMP ® method (Other)
结局指标
主要结局
USP (Urinary Symptoms Profile) score
时间窗: 38 weeks
Urinary Symptoms Profile score
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
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